Asymmetric oxohydroxylation of α-alkyl enoates with potassium permanganate catalyzed by monocationic quaternary...
Buchler Glossary
Cinchonine (CAS-No. 118-10-5), a pseudoenantiomer of Cinchonidine, is a well-known chiral compound widely used as a racemic resolution agent since decades. Apart from this application Cinchonine and its Cinchona alkaloid derivatives acts as an efficient enantioselective organocatalyst in a wide variety of asymmetric reactions. Multiple examples can be reviewed in our free of charge chiral catalyst search data base. Nowadays, the term asymmetric oganocatalysis covers a wide range of organic processes and methodologies, providing efficient and environmentally friendly access to enantiomerically pure compounds. Cinchonine is a versatile tool in applied Green Chemistry.
Find other examples of Chiral Organocatalysts in the Buchler Chiral Catalyst Database.
Further Articles:
(DHQ)2PHAL (CAS-No. 140924-50-1)
(DHQ)2PHAL - Dihydroquinine 1,4-phthalazinediyl diether (CAS-No. 140924-50-1) The well-known Cinchona alkaloid...
(DHQD)2PHAL (CAS-No. 140853-10-7)
(DHQD)2PHAL - Dihydroquinidine 1,4-phthalazinediyl diether (CAS-No. 140853-10-7) The well-known Cinchona alkaloid...
1,2-Addition
1,2-Addition is a type of organic chemical reaction that involves the addition of functional groups to the 1st and 2nd...
1,4-Addition (conjugate addition)
The Michael reaction is the conjugate 1,4-Addition of a resonance stabilized carbanion (michael donor) to an activated...
6`-Aminocinchonine (CAS-No. 2143936-31-4)
6´-Aminocinchonine Base (CAS-No. 2143936-31-4), a pseudoenantiomer of 6´-Aminocinchonidine, has the same...